Literature DB >> 23464572

Breeding research on sake yeasts in Japan: history, recent technological advances, and future perspectives.

Hiroshi Kitagaki1, Katsuhiko Kitamoto.   

Abstract

Sake is an alcoholic beverage of Japan, with a tradition lasting more than 1,300 years; it is produced from rice and water by fermenting with the koji mold Aspergillus oryzae and sake yeast Saccharomyces cerevisiae. Breeding research on sake yeasts was originally developed in Japan by incorporating microbiological and genetic research methodologies adopted in other scientific areas. Since the advent of a genetic paradigm, isolation of yeast mutants has been a dominant approach for the breeding of favorable sake yeasts. These sake yeasts include (a) those that do not form foams (produced by isolating a mutant that does not stick to foams, thus decreasing the cost of sake production); (b) those that do not produce urea, which leads to the formation of ethyl carbamate, a possible carcinogen (isolated by positive selection in a canavanine-, arginine-, and ornithine-containing medium); (c) those that produce an increased amount of ethyl caproate, an apple-like flavor (produced by isolating a mutant resistant to cerulenin, an inhibitor of fatty-acid synthesis); and (d) those that produce a decreased amount of pyruvate (produced by isolating a mutant resistant to an inhibitor of mitochondrial transport, thus decreasing the amount of diacetyl). Given that sake yeasts perform sexual reproduction, sporulation and mating are potent approaches for their breeding. Recently, the genome sequences of sake yeasts have been determined and made publicly accessible. By utilizing this information, the quantitative trait loci (QTLs) for the brewing characteristics of sake yeasts have been identified, which paves a way to DNA marker-assisted selection of the mated strains. Genetic engineering technologies for experimental yeast strains have recently been established by academic groups, and these technologies have also been applied to the breeding of sake yeasts. Sake yeasts whose genomes have been modified with these technologies correspond to genetically modified organisms (GMOs). However, technologies that enable the elimination of extraneous DNA sequences from the genome of sake yeast have been developed. Sake yeasts genetically modified with these technologies are called self-cloning yeasts and do not contain extraneous DNA sequences. These yeasts were exempted from the Japanese government's guidelines for genetically modified food. Protoplast fusion has also been utilized to breed favorable sake yeasts. Future directions for the breeding of sake yeasts are also proposed in this review. The reviewed research provides perspectives for the breeding of brewery yeasts in other fermentation industries.

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Year:  2013        PMID: 23464572     DOI: 10.1146/annurev-food-030212-182545

Source DB:  PubMed          Journal:  Annu Rev Food Sci Technol        ISSN: 1941-1421


  24 in total

1.  Indigenous bacteria and fungi drive traditional kimoto sake fermentations.

Authors:  Nicholas A Bokulich; Moe Ohta; Morgan Lee; David A Mills
Journal:  Appl Environ Microbiol       Date:  2014-06-27       Impact factor: 4.792

2.  Bacterial DNA Detected in Japanese Rice Wines and the Fermentation Starters.

Authors:  Momoka Terasaki; Akari Fukuyama; Yurika Takahashi; Masato Yamada; Hiromi Nishida
Journal:  Curr Microbiol       Date:  2017-08-22       Impact factor: 2.188

3.  Glucosylceramide Contained in Koji Mold-Cultured Cereal Confers Membrane and Flavor Modification and Stress Tolerance to Saccharomyces cerevisiae during Coculture Fermentation.

Authors:  Kazutaka Sawada; Tomoya Sato; Hiroshi Hamajima; Lahiru Niroshan Jayakody; Miyo Hirata; Mikako Yamashiro; Marie Tajima; Susumu Mitsutake; Koji Nagao; Keisuke Tsuge; Fumiyoshi Abe; Kentaro Hanada; Hiroshi Kitagaki
Journal:  Appl Environ Microbiol       Date:  2015-03-20       Impact factor: 4.792

4.  Robust Domination of Lactobacillus sakei in Microbiota During Traditional Japanese Sake Starter Yamahai-Moto Fermentation and the Accompanying Changes in Metabolites.

Authors:  Atsushi Tsuji; Miyuki Kozawa; Koji Tokuda; Toshiki Enomoto; Takashi Koyanagi
Journal:  Curr Microbiol       Date:  2018-08-16       Impact factor: 2.188

Review 5.  Lager yeast comes of age.

Authors:  Jürgen Wendland
Journal:  Eukaryot Cell       Date:  2014-08-01

Review 6.  Improving industrial yeast strains: exploiting natural and artificial diversity.

Authors:  Jan Steensels; Tim Snoek; Esther Meersman; Martina Picca Nicolino; Karin Voordeckers; Kevin J Verstrepen
Journal:  FEMS Microbiol Rev       Date:  2014-05-08       Impact factor: 16.408

7.  Nutrient Signaling via the TORC1-Greatwall-PP2AB55δ Pathway Is Responsible for the High Initial Rates of Alcoholic Fermentation in Sake Yeast Strains of Saccharomyces cerevisiae.

Authors:  Daisuke Watanabe; Takuma Kajihara; Yukiko Sugimoto; Kenichi Takagi; Megumi Mizuno; Yan Zhou; Jiawen Chen; Kojiro Takeda; Hisashi Tatebe; Kazuhiro Shiozaki; Nobushige Nakazawa; Shingo Izawa; Takeshi Akao; Hitoshi Shimoi; Tatsuya Maeda; Hiroshi Takagi
Journal:  Appl Environ Microbiol       Date:  2018-12-13       Impact factor: 4.792

8.  Chromosomal Aneuploidy Improves the Brewing Characteristics of Sake Yeast.

Authors:  Masafumi Kadowaki; Yuki Fujimaru; Seiga Taguchi; Jannatul Ferdouse; Kazutaka Sawada; Yuta Kimura; Yohei Terasawa; Gennaro Agrimi; Toyoaki Anai; Hideki Noguchi; Atsushi Toyoda; Asao Fujiyama; Takeshi Akao; Hiroshi Kitagaki
Journal:  Appl Environ Microbiol       Date:  2017-12-01       Impact factor: 4.792

9.  Enhancement of ethanol fermentation in Saccharomyces cerevisiae sake yeast by disrupting mitophagy function.

Authors:  Shodai Shiroma; Lahiru Niroshan Jayakody; Kenta Horie; Koji Okamoto; Hiroshi Kitagaki
Journal:  Appl Environ Microbiol       Date:  2013-11-22       Impact factor: 4.792

10.  Genome Editing to Generate Sake Yeast Strains with Eight Mutations That Confer Excellent Brewing Characteristics.

Authors:  Tomoya Chadani; Shinsuke Ohnuki; Atsuko Isogai; Tetsuya Goshima; Mao Kashima; Farzan Ghanegolmohammadi; Tomoyuki Nishi; Dai Hirata; Daisuke Watanabe; Katsuhiko Kitamoto; Takeshi Akao; Yoshikazu Ohya
Journal:  Cells       Date:  2021-05-24       Impact factor: 6.600

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